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A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Blocking a protein called prostaglandin D2 might help treat hair loss.

Amino acid storage proteins are essential for maintaining stem cells in female fruit flies.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

2-DG reduces seizures by enhancing brain inhibition through specific receptor activation.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

PGD2 stops hair growth and is higher in bald men with AGA.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A new mouse model helps study melanocyte cells using GFP expression.

The Gsdma3 gene is essential for normal hair development in mice.